"70934-885-30" National Drug Code (NDC)

NDC Code	70934-885-30
Package Description	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-885-30)
Product NDC	70934-885
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Chloride
Non-Proprietary Name	Potassium Chloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20210824
End Marketing Date	20230630
Marketing Category Name	ANDA
Application Number	ANDA076368
Manufacturer	Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance Name	POTASSIUM CHLORIDE
Strength	20
Strength Unit	meq/1
Pharmacy Classes	Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]